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Tianish Laboratories in Hyderabad, R&D Centre, invites a qualified professional to lead analytical method validation activities. The role requires strong experience in validation protocols, regulatory support, and method transfer execution within a GMP/GLP framework.
You will contribute to regulatory documentation, ensure adherence to safety standards, and collaborate with the ARD - Method Validation team in a fast-paced research environment.
Qualification: Master of Science/Master of Pharmacy
Experience: 8 14 Years
Department: ARD - Method Validation
Location: Hyderabad, R&D Centre